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NEXWAVE COMBO MUSCLE STIMULATOR SYSTEM

K111279 Class II Abbreviated
Decision Date
2011-09-20
Sponsor / Applicant
Zynex Medical, Inc.

Technical Specification

510(k) Submission ID K111279
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 2011-09-20
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEXWAVE COMBO MUSCLE STIMULATOR SYSTEM received FDA 510(k) clearance under submission number K111279, sponsored by Zynex Medical, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2011-09-20.

Classification & Regulation

This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.